Menon Darsan B, Gopalakrishnan V K
a Department of Biotechnology , Karpagam University , Coimbatore , Tamilnadu , India.
Nutr Cancer. 2015;67(4):697-705. doi: 10.1080/01635581.2015.1019631. Epub 2015 Apr 2.
The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cell death induction by the terpenoid fraction on human colon cancer cells (HCT-15). MTT assay was performed with different concentrations of the fraction (10, 20, and 50 µg/mL) to obtain IC50 value for 24 h to induce cell death. The induction of apoptosis were studied by Hoechst staining, acridine orange/ethidium bromide staining, Comet assay, DNA fragmentation, and caspase-3 activity assays. The mechanism of apoptosis induction was studied by expression analysis of antiapoptotic Bcl-2 and proapoptotic Bax using RT-PCR and also by Western blot analysis of proteins involved in the apoptotic pathway. The terpenoid fraction induced significant morphological changes and DNA fragmentation in the cells. Positive Hoechst staining and acridine orange/ethidium bromide staining indicated apoptosis induction by the fraction. DNA fragmentation, which is a characteristic feature of apoptosis, was also observed. Upregulation of caspase-3 activity and proapoptotic Bax, and the downregulation of antiapoptotic Bcl-2 and COX-2 confirmed that the apoptosis induction was via the mitochondria-dependent pathway.
植物哈氏香茶菜是多种生物活性植物化学物质的丰富来源,尤其是萜类化合物。分离出萜类部分,并使用气相色谱 - 质谱联用仪进行植物化学表征。本研究的目的是探究萜类部分对人结肠癌细胞(HCT - 15)的抗增殖活性和诱导细胞死亡的机制。用不同浓度的该部分(10、20和50 µg/mL)进行MTT试验,以获得24小时诱导细胞死亡的IC50值。通过Hoechst染色、吖啶橙/溴化乙锭染色、彗星试验、DNA片段化和caspase - 3活性测定来研究细胞凋亡的诱导情况。通过使用逆转录 - 聚合酶链反应对抗凋亡蛋白Bcl - 2和促凋亡蛋白Bax进行表达分析,以及对凋亡途径中涉及的蛋白质进行蛋白质印迹分析,来研究凋亡诱导的机制。萜类部分在细胞中诱导了显著的形态变化和DNA片段化。Hoechst染色阳性和吖啶橙/溴化乙锭染色表明该部分诱导了细胞凋亡。还观察到了作为细胞凋亡特征的DNA片段化。caspase - 3活性和促凋亡蛋白Bax的上调,以及抗凋亡蛋白Bcl - 2和COX - 2的下调证实了凋亡诱导是通过线粒体依赖性途径进行的。